Clinical Research Associate (CRA) Full service/ Multisponsor
IQVIA
Athens, Greece
πριν από 22 ώρες

Whether you’re beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You’ll have training and development to plan and progress your career in the direction you choose.

And you won’t do it alone you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.

While Projects Vary, Your Typical Responsibilities Might Include

  • Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
  • Supporting the development of a subject recruitment plan
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
  • Evaluating the quality and integrity of site practices escalating quality issues as appropriate
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
  • You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.

    You Should Have

  • A Bachelor's degree in a health care or other scientific discipline or educational equivalent
  • At least 1 year of on-site monitoring experience
  • Good written and verbal communication skills including good command of English language
  • Requires frequent travel to sites
  • Flexible about location, but location must have good connectivity to travel
  • Homebased
  • If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team .

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